US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 27, 2022 (4 years ago)

Launch Sequence Capsules

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.

What was recalled

Launch Sequence Capsules, Dietary Supplement, 60- count bottles, ASIN B07TLPWXDS, UPC Code 641378938375.

Recalling firm
Loud Muscle Science
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1339-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.